首页> 外文期刊>BioChip journal >Droplet-based Microfluidics for Making Uniform-sized Cellular Spheroids in Alginate Beads with the Regulation of Encapsulated Cell Number
【24h】

Droplet-based Microfluidics for Making Uniform-sized Cellular Spheroids in Alginate Beads with the Regulation of Encapsulated Cell Number

机译:基于微滴的微流控技术,可在藻酸盐微珠中制备均一尺寸的细胞球体,并具有封装细胞数的调节作用

获取原文
获取原文并翻译 | 示例
       

摘要

Droplet-based microfluidic devices are a promising strategy for generating highly-reproducible, massive cellular spheroids. However, there were challenges in the previously-reported microencapsulation device for forming uniformly-sized cellular spheroids because of difficulty in regulating the number of encapsulated cells in the alginate beads. Here, I introduce an advanced droplet-based microfluidic device that is capable of generating the number of encapsulated cells in a more uniform fashion than the previously-reported microencapsulation device via dispersing cell clusters formed by self-assembly into an individual single cell at a cell-scattering component. When cell clusters were introduced in the cell scattering component, the initial large-sized cell clusters were scattered into single cells via about 10 iterations of sequential processes (split, stretch, and bump). After cell encapsulation, the number of encapsulated cells coincided with the Poisson distribution in the cell-scattering encapsulation device, while the number of encapsulated cells was rather randomized in the previous device; the cell clusters were encapsulated in 20% of all alginate beads. In addition, more uniform-sized cellular spheroids were generated in the beads by the cell-scattering encapsulation than by the previously-reported device via adjusting the number of cells in the beads. The proposed method provides a valuable tool for generating massive and uniform cellular spheroids, which will contribute to the development of a new quantitative analysis of stem cell differentiation and cancer research.
机译:基于液滴的微流体装置是产生高度可重现的大量细胞球体的有前途的策略。然而,由于难以调节藻酸盐珠粒中包封细胞的数目,因此在先前报道的用于形成均一大小的细胞球体的微囊化装置中存在挑战。在这里,我介绍一种先进的基于液滴的微流控设备,该设备能够通过将自组装形成的细胞簇分散到一个细胞中的单个单个细胞中,从而以比以前报告的微囊化设备更均匀的方式生成被囊化细胞的数量。 -散射组件。当将细胞簇引入细胞散射组件中时,最初的大型细胞簇通过约10次连续的迭代过程(分裂,拉伸和碰撞)分散成单个细胞。细胞封装后,封装细胞的数量与细胞散射封装设备中的泊松分布相符,而封装设备的数量在先前的设备中相当随机。细胞簇被封装在所有藻酸盐珠粒的20%中。另外,通过调节细胞内的细胞数量,通过细胞散射封装在珠子中产生了比以前报道的装置更均匀大小的细胞球体。所提出的方法为生成大量且均匀的细胞球体提供了有价值的工具,这将有助于干细胞分化和癌症研究的新定量分析方法的发展。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号